CACNA1F and CABP4

Number of citations of the paper that reports this interaction (PubMedID 15452577)
50

Data Source:
HPRD (in vitro)

		CACNA1F	CABP4
Description		calcium voltage-gated channel subunit alpha1 F	calcium binding protein 4
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Photoreceptor Outer Segment Voltage-gated Calcium Channel Complex Membrane Monoatomic Ion Channel Complex Neuronal Cell Body Perikaryon	Extracellular Region Cytoplasm Cytosol Cell Projection Terminal Bouton Synapse Presynapse
	Molecular Function	Monoatomic Ion Channel Activity Voltage-gated Calcium Channel Activity Calcium Channel Activity Protein Binding High Voltage-gated Calcium Channel Activity Metal Ion Binding	Calcium Channel Regulator Activity Calcium Ion Binding Transmembrane Transporter Binding Metal Ion Binding
	Biological Process	Monoatomic Ion Transport Calcium Ion Transport Visual Perception Monoatomic Ion Transmembrane Transport Detection Of Light Stimulus Involved In Visual Perception Transmembrane Transport Calcium Ion Transmembrane Transport Calcium Ion Import Across Plasma Membrane Negative Regulation Of Voltage-gated Calcium Channel Activity	Signal Transduction Visual Perception Phototransduction Photoreceptor Cell Morphogenesis Retinal Cone Cell Development Retinal Bipolar Neuron Differentiation
Pathways
Drugs		Ergocalciferol Enflurane Ranolazine Phenytoin Topiramate Nimodipine Spironolactone Cinnarizine Nicardipine Magnesium sulfate Verapamil Levomenthol Nitrendipine Miconazole Amiodarone Mibefradil Dronedarone Clevidipine Nilvadipine Drotaverine Trimebutine Aranidipine Benidipine Cilnidipine Efonidipine Efonidipine Lacidipine Manidipine Butamben Bioallethrin Bioallethrin Fish oil
Diseases		Congenital stationary night blindness (CSNB), including: CSNB type 1 (CSNB1); CSNB type 2 (CSNB2); CSNB autosomal dominant (CSNBAD); Oguchi disease/ CSNB Oguchi type (CSNBO) Aland Island eye disease; Forsius-Eriksson syndrome Cone-rod dystrophy and cone dystrophy, including: Cone-rod dystrophy (CORD); Cone dystrophy (COD); Retinal cone dystrophy (RCD)	Congenital stationary night blindness (CSNB), including: CSNB type 1 (CSNB1); CSNB type 2 (CSNB2); CSNB autosomal dominant (CSNBAD); Oguchi disease/ CSNB Oguchi type (CSNBO)
GWAS			Mean corpuscular volume ( 27863252 32888494) Mean reticulocyte volume ( 32888494) Refractive error ( 32231278)
Interacting Genes		1 interacting genes: CABP4	7 interacting genes: BCL6 CACNA1F IKZF3 LNX2 MFHAS1 PACS1 TLE5
Entrez ID		778	57010
HPRD ID		02119	12344
Ensembl ID		ENSG00000102001	ENSG00000175544
Uniprot IDs		O60840	P57796
PDB IDs
Enriched GO Terms of Interacting Partners?		Photoreceptor Cell Morphogenesis Retinal Cone Cell Development Retinal Bipolar Neuron Differentiation Glutamatergic Neuron Differentiation Cell Morphogenesis Involved In Neuron Differentiation Photoreceptor Cell Development Terminal Bouton Eye Photoreceptor Cell Development Phototransduction Calcium Channel Regulator Activity Detection Of Light Stimulus Detection Of Abiotic Stimulus Transmembrane Transporter Binding Visual Perception Cell Morphogenesis Sensory Perception Of Light Stimulus Neuron Development Presynapse Detection Of Stimulus Response To Light Stimulus Neuron Differentiation
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